Teikyo University Institute of Medical Mycology , Hachioji, Tokyo, Japan.
Division of Infection and Immunity, Research Center for Zoonosis Control, Hokkaido University , Sapporo, Japan.
Virulence. 2021 Dec;12(1):470-480. doi: 10.1080/21505594.2021.1875683.
We previously reported that disruption of the gene reduced virulence of . In this study, we found virulence in both silkworms and mice was restored by introducing the gene but not the gene to both and genes-disrupted mutants, suggesting that , the gene downstream to the gene in a two-gene operon-, is responsible for this phenomenon. We further observed a decrease in various surface-associated proteins and changes in cell envelope glycostructures in the mutants. RNA-seq analysis revealed that disruption of the and the genes resulted in differential expression of a broad range of genes, notably, significant downregulation of genes involved in virulence and oxidative stress. Administration of N-acetyl-L-cysteine, a free-radical scavenger, restored the virulence in both the mutants. Our findings suggested that YjbH plays a role in staphylococcal pathogenicity by regulating virulence gene expression, affecting the bacterial surface structure, and conferring resistance to oxidative stress in a host.
我们之前的研究表明,基因的缺失会降低的毒力。在本研究中,我们发现通过向两个基因缺失突变体引入基因而不是基因,可以恢复家蚕和小鼠中的毒力,这表明基因下游的基因在双基因操纵子中,是负责这一现象的基因。我们进一步观察到突变体中各种表面相关蛋白减少和细胞包膜糖结构发生变化。RNA-seq 分析表明,基因和基因的缺失导致广泛基因的差异表达,特别是与毒力和氧化应激相关的基因显著下调。自由基清除剂 N-乙酰-L-半胱氨酸的给药可恢复两个突变体的毒力。我们的研究结果表明,YjbH 通过调节毒力基因表达、影响细菌表面结构以及在宿主中赋予对氧化应激的抗性,在葡萄球菌致病性中发挥作用。